ALOMONE LABS Non-Antibody Products — page 9 of 47
Non-Antibody Products
Page 9 of 47
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Bradykinin | Bradykinin is an endothelial dependent vasodilator and hypotensive agent1.… | 25 mg | GPB-200 | More Info |
| Bradykinin | Bradykinin is an endothelial dependent vasodilator and hypotensive agent1.… | 5 mg | GPB-200 | More Info |
| Bradykinin | Bradykinin is an endothelial dependent vasodilator and hypotensive agent1.… | 50 mg | GPB-200 | More Info |
| Bradykinin | Bradykinin is an endothelial dependent vasodilator and hypotensive agent1.… | 500 mg | GPB-200 | More Info |
| Brefeldin A | Brefeldin A is an antiviral antibiotic which inhibits protein transport fr… | 5 x 1 mg | B-275 | More Info |
| Brefeldin A | Brefeldin A is an antiviral antibiotic which inhibits protein transport fr… | 1 mg | B-275 | More Info |
| Bupivacaine hydrochloride | Bupivacaine blocks both TTX-sensitive and TTX-resistant NaV channels in DR… | 1 g | B-125 | More Info |
| Bupivacaine hydrochloride | Bupivacaine blocks both TTX-sensitive and TTX-resistant NaV channels in DR… | 15 g | B-125 | More Info |
| Bupivacaine hydrochloride | Bupivacaine blocks both TTX-sensitive and TTX-resistant NaV channels in DR… | 5 g | B-125 | More Info |
| BzATP triethylammonium salt | BzATP triethylammonium salt is an agonist of the purinergic P2X7 receptor,… | 10 mg | A-385 | More Info |
| BzATP triethylammonium salt | BzATP triethylammonium salt is an agonist of the purinergic P2X7 receptor,… | 25 mg | A-385 | More Info |
| BzATP triethylammonium salt | BzATP triethylammonium salt is an agonist of the purinergic P2X7 receptor,… | 5 mg | A-385 | More Info |
| BzATP triethylammonium salt | BzATP triethylammonium salt is an agonist of the purinergic P2X7 receptor,… | 6 g | A-385 | More Info |
| Caffeine | RYR activator. Purity ≥99%. MW: 194.19 | 500 mg | C-395 | More Info |
| Calcicludine | Calcicludine is a potent and specific antagonist of neuronal L-type CaV ch… | 0.25 mg | SPC-650 | More Info |
| Calcicludine | Calcicludine is a potent and specific antagonist of neuronal L-type CaV ch… | 0.5 mg | SPC-650 | More Info |
| Calcicludine | Calcicludine is a potent and specific antagonist of neuronal L-type CaV ch… | 1 mg | SPC-650 | More Info |
| Calcicludine | Calcicludine is a potent and specific antagonist of neuronal L-type CaV ch… | 10 mg | SPC-650 | More Info |
| Calcicludine | Calcicludine is a potent and specific antagonist of neuronal L-type CaV ch… | 5 mg | SPC-650 | More Info |
| Calcicludine | Calcicludine is a potent and specific antagonist of neuronal L-type CaV ch… | 70 µg | SPC-650 | More Info |
| Calcicludine | Calcicludine is a potent and specific antagonist of neuronal L-type CaV ch… | 70 µg - Free Sample | SPC-650 | More Info |
| Calciseptine | Calciseptine is a specific antagonist of L-type CaV channels1. Synthetic p… | 0.25 mg | SPC-500 | More Info |
| Calciseptine | Calciseptine is a specific antagonist of L-type CaV channels1. Synthetic p… | 0.5 mg | SPC-500 | More Info |
| Calciseptine | Calciseptine is a specific antagonist of L-type CaV channels1. Synthetic p… | 1 mg | SPC-500 | More Info |
| Calciseptine | Calciseptine is a specific antagonist of L-type CaV channels1. Synthetic p… | 10 mg | SPC-500 | More Info |
| Calciseptine | Calciseptine is a specific antagonist of L-type CaV channels1. Synthetic p… | 5 mg | SPC-500 | More Info |
| Calciseptine | Calciseptine is a specific antagonist of L-type CaV channels1. Synthetic p… | 70 µg | SPC-500 | More Info |
| Calciseptine | Calciseptine is a specific antagonist of L-type CaV channels1. Synthetic p… | 70 µg - Free Sample | SPC-500 | More Info |
| Calyculin A | Calyculin A is a very potent, cell-permeable PP-1 and PP-2 inhibitor (IC50… | 0.1 mg | C-100 | More Info |
| Calyculin A | Calyculin A is a very potent, cell-permeable PP-1 and PP-2 inhibitor (IC50… | 10 µg | C-100 | More Info |
| Calyculin A | Calyculin A is a very potent, cell-permeable PP-1 and PP-2 inhibitor (IC50… | 25 µg | C-100 | More Info |
| Calyculin A | Calyculin A is a very potent, cell-permeable PP-1 and PP-2 inhibitor (IC50… | 50 µg | C-100 | More Info |
| Camptothecin | Camptothecin is an alkaloid that specifically inhibits DNA topoisomerase I… | 100 mg | C-330 | More Info |
| Camptothecin | Camptothecin is an alkaloid that specifically inhibits DNA topoisomerase I… | 250 mg | C-330 | More Info |
| Camptothecin | Camptothecin is an alkaloid that specifically inhibits DNA topoisomerase I… | 50 mg | C-330 | More Info |
| Camptothecin | Camptothecin is an alkaloid that specifically inhibits DNA topoisomerase I… | 500 mg | C-330 | More Info |
| Candesartan | Candesartan is an Angiotensin II type 1 and 2 receptor antagonist1,2. Synt… | 1 g | C-266 | More Info |
| Candesartan | Candesartan is an Angiotensin II type 1 and 2 receptor antagonist1,2. Synt… | 100 mg | C-266 | More Info |
| Candesartan | Candesartan is an Angiotensin II type 1 and 2 receptor antagonist1,2. Synt… | 50 mg | C-266 | More Info |
| Candesartan | Candesartan is an Angiotensin II type 1 and 2 receptor antagonist1,2. Synt… | 500 mg | C-266 | More Info |
| Candesartan cilexetil | Candesartan is an Angiotensin II type 1 and 2 receptor antagonist1,2. Synt… | 1 g | C-265 | More Info |
| Candesartan cilexetil | Candesartan is an Angiotensin II type 1 and 2 receptor antagonist1,2. Synt… | 10 g | C-265 | More Info |
| Candesartan cilexetil | Candesartan is an Angiotensin II type 1 and 2 receptor antagonist1,2. Synt… | 250 mg | C-265 | More Info |
| Candesartan cilexetil | Candesartan is an Angiotensin II type 1 and 2 receptor antagonist1,2. Synt… | 5 g | C-265 | More Info |
| Candesartan cilexetil | Candesartan is an Angiotensin II type 1 and 2 receptor antagonist1,2. Synt… | 500 mg | C-265 | More Info |
| Cannabichromene | CBC is an activator of TRPA1 with an EC50 of 90 nM and a blocker of TRPM8… | 10 mg | C-315 | More Info |
| Cannabichromene | CBC is an activator of TRPA1 with an EC50 of 90 nM and a blocker of TRPM8… | 25 mg | C-315 | More Info |
| Cannabichromene | CBC is an activator of TRPA1 with an EC50 of 90 nM and a blocker of TRPM8… | 5 mg | C-315 | More Info |
| Cannabichromene | CBC is an activator of TRPA1 with an EC50 of 90 nM and a blocker of TRPM8… | 1 mg | C-315 | More Info |
| Cannabidiol | Cannabidiol is an activator of TRPV1, TRPV3 and TRPA1 channels1. Natural.… | 100 mg | C-320 | More Info |
| Cannabidiol | Cannabidiol is an activator of TRPV1, TRPV3 and TRPA1 channels1. Natural.… | 25 mg | C-320 | More Info |
| Cannabidiol | Cannabidiol is an activator of TRPV1, TRPV3 and TRPA1 channels1. Natural.… | 5 mg | C-320 | More Info |
| Cannabidiol | Cannabidiol is an activator of TRPV1, TRPV3 and TRPA1 channels1. Natural.… | 50 mg | C-320 | More Info |
| Cannabidiol | Cannabidiol is an activator of TRPV1, TRPV3 and TRPA1 channels1. Natural.… | 10 mg | C-320 | More Info |
| Cantharidic Acid | Cantharidic acid is a potent inhibitor of PP1 and PP2A (IC50 = 50 nM)1,2.… | 1 mg | C-250 | More Info |
| Cantharidic Acid | Cantharidic acid is a potent inhibitor of PP1 and PP2A (IC50 = 50 nM)1,2.… | 5 x 1 mg | C-250 | More Info |
| Cantharidin | Cantharidin is a potent inhibitor of PP1 and PP2A (IC50 = 1.7 and 0.16 &mi… | 10 mg | C-170 | More Info |
| Cantharidin | Cantharidin is a potent inhibitor of PP1 and PP2A (IC50 = 1.7 and 0.16 &mi… | 100 mg | C-170 | More Info |
| Cantharidin | Cantharidin is a potent inhibitor of PP1 and PP2A (IC50 = 1.7 and 0.16 &mi… | 25 mg | C-170 | More Info |
| Cantharidin | Cantharidin is a potent inhibitor of PP1 and PP2A (IC50 = 1.7 and 0.16 &mi… | 5 mg | C-170 | More Info |
| Cantharidin | Cantharidin is a potent inhibitor of PP1 and PP2A (IC50 = 1.7 and 0.16 &mi… | 5 x 1 mg | C-170 | More Info |
| Cantharidin | Cantharidin is a potent inhibitor of PP1 and PP2A (IC50 = 1.7 and 0.16 &mi… | 50 mg | C-170 | More Info |
| Cantharidin | Cantharidin is a potent inhibitor of PP1 and PP2A (IC50 = 1.7 and 0.16 &mi… | 1 mg | C-170 | More Info |
| Capsaicin | Capsaicin is one of the most powerful chemical agonists of the TRPV1 (tran… | 1 g | C-125 | More Info |
| Capsaicin | Capsaicin is one of the most powerful chemical agonists of the TRPV1 (tran… | 100 mg | C-125 | More Info |
| Capsaicin | Capsaicin is one of the most powerful chemical agonists of the TRPV1 (tran… | 250 mg | C-125 | More Info |
| Capsaicin | Capsaicin is one of the most powerful chemical agonists of the TRPV1 (tran… | 50 mg | C-125 | More Info |
| Capsaicin | Capsaicin is one of the most powerful chemical agonists of the TRPV1 (tran… | 500 mg | C-125 | More Info |
| Capsazepine | Capsazepine is a selective antagonist of the vanilloid VR1 receptor (TRPV1… | 10 mg | C-120 | More Info |
| Capsazepine | Capsazepine is a selective antagonist of the vanilloid VR1 receptor (TRPV1… | 25 mg | C-120 | More Info |
| Capsazepine | Capsazepine is a selective antagonist of the vanilloid VR1 receptor (TRPV1… | 5 mg | C-120 | More Info |
| Capsazepine | Capsazepine is a selective antagonist of the vanilloid VR1 receptor (TRPV1… | 50 mg | C-120 | More Info |
| Capsiate | Capsiate activates TRPV1 and TRPA1 channels with EC50 = 3 µM1. Natur… | 25 mg | C-255 | More Info |
| Capsiate | Capsiate activates TRPV1 and TRPA1 channels with EC50 = 3 µM1. Natur… | 5 mg | C-255 | More Info |
| Capsiate | Capsiate activates TRPV1 and TRPA1 channels with EC50 = 3 µM1. Natur… | 10 mg | C-255 | More Info |
ALOMONE LABS
ALOMONE LABS
Jerusalem BioPark (JBP), Hadassah Ein Kerem
PO Box 4287
Jerusalem, 9104201 ISRAEL
P: +972-2-587-2202
F: +972-2-587-1101
info@alomone.com
http://www.alomone.com
U.S.A. OFFICE
Toll free phone: 1800-618-1644 / 1800-791-3904
Toll free fax: 1888-454-7276 / 1800-791-3912
Return to Profile